Canonical Allele Identifier: PA2826313331
Gene: SNCAIP HGNC NCBI

Linked Data

ClinVar Variation Id: 904533
ClinVar RCV Id: RCV001152512
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229864.1:p.Ala281Pro
CA3385007
NM_001242935.3:c.841G>C